Showing results (1881-1890 of 9,792) with videos related to
Sort By:
Pageof 980
American Journal of Human Genetics|November 4, 2017
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual DisabilitySébastien Küry, Geeske M van Woerden, Thomas Besnard, et al.American Journal of Human Genetics|February 1, 1989
Identifying pedigrees segregating at a major locus for a quantitative trait: an efficient strategy for linkage analysisM Boehnke, P P MollAmerican Journal of Human Genetics|December 9, 2017
De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait AbnormalitiesSonja Martin, Adam Chamberlin, Deepali N Shinde, et al.American Journal of Human Genetics|March 1, 1989
Linkage disequilibrium, cystic fibrosis, and genetic counselingA L Beaudet, G L Feldman, S D Fernbach, et al.American Journal of Human Genetics|March 1, 1989
Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6N G Kennaway, L Stankova, M K Wirtz, et al.American Journal of Human Genetics|March 1, 1989
Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasiaW L Bigbee, R G Langlois, M Swift, et al.American Journal of Human Genetics|March 1, 1989
Heritability of bone mass: a longitudinal study in aging male twinsJ C Christian, P L Yu, C W Slemenda, et al.American Journal of Human Genetics|September 5, 2017
Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated GenesStefan H Lelieveld, Laurens Wiel, Hanka Venselaar, et al.American Journal of Human Genetics|September 5, 2017
Exonic Mosaic Mutations Contribute Risk for Autism Spectrum DisorderDeidre R Krupp, Rebecca A Barnard, Yannis Duffourd, et al.American Journal of Human Genetics|September 9, 2017
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in FibrosisMichael Ng, Dipti Thakkar, Lorraine Southam, et al.Pageof 980